Project Manager/Senior Project (12-month parental leave cover)

Posted 2 Days Ago
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Glostrup, Hovedstaden, DNK
In-Office
Mid level
Biotech
The Role
The Project Manager will lead IVDR transition projects for cancer diagnostic products, coordinating cross-functional teams, managing budgets, and ensuring compliance with regulations.
Summary Generated by Built In
Job Description

Background 

Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the answers and insights they seek - so they can do what they do best: improve the world around us. Information about Agilent is available at www.agilent.com. 

 

Join us in the fight against cancer 

Are you a project manager passionate about playing a key role in advancing cancer diagnostics? Or do you bring expertise in IVD or medical devices and want to step into project leadership? 

 

We are looking for a Project Manager / Senior Project Manager to join our In Vitro Diagnostic Regulation (IVDR) Program Office in Glostrup, Denmark, where you will play a key role in transitioning Agilent’s pathology portfolio to compliance with the European Regulation on in vitro diagnostics. 

 

This is a unique opportunity to contribute directly to the availability of high-quality cancer diagnostics for patients worldwide. 

 

Your Main Responsibilities will be: 

  • Lead one or more IVDR transition projects for cancer diagnostic products. This may include delivery of technical file documentation, submission to a notified body, and ensuring manufacturing readiness. 

  • Develop project plans, budgets, and resource plans in collaboration with stakeholders. 

  • Lead geographically diverse, cross-functional project teams, including, but not limited to, Marketing, Research and Development, Regulatory, Quality Assurance, and Manufacturing. 

  • Monitor project progress and communicate status, risks, and mitigation plans to stakeholders 

  • Manage risks, dependencies, and cross-project interfaces 

  • Proactively resolve challenges and drive decision-making 

  • Foster alignment, accountability, and engagement within project teams

Qualifications

We are looking for a motivated individual with the following background: 

 

  • A relevant Master’s background related to Life Science or Engineering. 

  • Experience with coordination of project teams and proven success in delivering results in a highly regulated industry. 

  • Solid understanding of working with design control documentation for in vitro diagnostic or medical devices. 

  • Strong collaboration, stakeholder management and communication skills to align and set direction for project teams 

  • Excellent English verbal/written communications skills. 

  • Problem solving, planning and analytical skills. 

  • Ability and flexibility to manage uncertainty, ambiguity, and changes in direction in a fast-paced work environment 

  • Knowledge of IVDR is a plus. 

  • Certification in Project Management (e.g. Prince2, IPMA, PMP etc.) is a plus. 

 

On a personal level, you demonstrate openness, proactivity, and a strong eagerness to learn. Your curiosity and problem-solving mindset drive you to seek innovative solutions. You are passionate about supporting and empowering others, and you confidently set direction when needed. At Agilent, you will have the opportunity to channel your curiosity and commitment to innovation, making a meaningful impact in a collaborative environment. 

 

 

We offer: 

  • The opportunity to be part of a dynamic team  

  • A role among passionate colleagues, in a growth orientated and inclusive environment. You will become part of a caring and fast paced environment, built on integrity, sharing and trust. 

  • A chance to be part of the lifecycle management of state-of-the-art diagnostic assays, benefiting cancer patients worldwide 

  • An international work environment 

  • A commitment to work/life balance.  

  • Career development opportunities in an international company. 

  • Competitive compensation and benefits package. 

Additional Details

This job has a full time weekly schedule.

Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.Travel Required: NoShift: DayDuration: 0-3 MonthsJob Function: R&D

Skills Required

  • A relevant Master's background related to Life Science or Engineering
  • Experience with coordination of project teams
  • Solid understanding of working with design control documentation for in vitro diagnostic or medical devices
  • Strong collaboration and stakeholder management skills
  • Excellent English verbal/written communication skills
  • Ability to manage uncertainty and changes in a fast-paced environment
  • Knowledge of IVDR
  • Certification in Project Management (e.g. Prince2, IPMA, PMP)

Agilent Technologies Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Agilent Technologies and has not been reviewed or approved by Agilent Technologies.

  • Retirement Support The core U.S. package highlights a generous 401(k) match as a strength. Retirement programs are positioned as competitive within the company’s total rewards.
  • Equity Value & Accessibility An Employee Stock Purchase Plan at a discount provides accessible equity and augments total compensation. Ownership opportunities are presented as a notable advantage alongside retirement benefits.
  • Leave & Time Off Breadth Flexible Time Off, company holidays, a personal holiday, and paid volunteer time create a broad leave offering. Time off can accrue into multiple weeks in the first year, supporting flexibility.

Agilent Technologies Insights

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The Company
HQ: Santa Clara, CA
17,369 Employees
Year Founded: 1999

What We Do

Analytical scientists and clinical researchers worldwide rely on Agilent to help fulfill their most complex laboratory demands. Our instruments, software, services and consumables address the full range of scientific and laboratory management needs—so our customers can do what they do best: improve the world around us. Whether a laboratory is engaged in environmental testing, academic research, medical diagnostics, pharmaceuticals, petrochemicals or food testing, Agilent provides laboratory solutions to meet their full spectrum of needs. We work closely with customers to help address global trends that impact human health and the environment, and to anticipate future scientific needs. Our solutions improve the efficiency of the entire laboratory, from sample prep to data interpretation and management. Customers trust Agilent for solutions that enable insights...for a better world.

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